Synthesis of α-Functionalized Allenes

It is known, since the work of Landor et al, that α-allenic alcohols can be specifically obtained by treating the monotetrahydropyranyl ether of a butyn-1,4-diol with lithium aluminium hydride (1). In this reaction, which can be also realized with another leaving group (halogen, ammonium) (2), the allenic linkage is formed by an S_N ^2′ process where the nucleophilic hydride is transferred from the initially formed alcoholate (scheme 1).     

Preparation and characterization of novel PES‐(SiO2‐g‐PMAA) membranes with antifouling and hydrophilic properties for separation of oil‐in‐water emulsions

In the present study, modification of nanoparticles (NPs) was investigated to mitigate aggregation of SiO₂ nanoparticles and improve the polymeric membrane's performance. For this purpose, the surface of SiO₂ nanoparticles was activated with amine groups, and polymethacrylic acid (PMAA) was grafted on the surface of NPs by atom transfer radical polymerization. Modified NPs were characterized by Fourier transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA) tests. Polyethersulfone (PES) membranes were fabricated with both SiO₂ and SiO₂‐g‐PMAA NPs via nonsolvent‐induced phase separation method. The fabricated membranes were characterized regarding their permeability, hydrophilicity, and porosity properties, and their separation efficiency was tested using the synthetic oil‐in‐water emulsion. The surface and cross‐sectional morphologies of membranes were observed by field emission scanning electron microscopy (FESEM). The experimental trials showed that modified NPs dispersed more uniformly in the structure of membranes and hydroxyl groups on the surface of NPs acted more effectively. Modification of NPs enhance the membrane performance in terms of permeate flux, hydrophilicity, and porosity. NPs modification improved the permeate flux about 46%. Oil rejection for all tested membranes was more than 98%, and modification of NPs did not reduce the rejection of membranes. The optimum concentration was obtained as 1 wt.% and 1.5 wt.% for SiO₂ and SiO₂‐g‐PMAA, respectively. Aggregation effect dominated at concentrations beyond the optimum values that decreased the permeate flux, consequently.     

The reactions of phenolic reagents with α-bromo Michael acceptors in the K2CO3-acetone system. A stereospecific AdSNE process.

α-bromo Michael acceptors undergo ipso-substitution by phenol or benzenethiol in the K₂CO₃-acetone system, the reaction originating the (Z) isomers, via a stereospecific Ad_SNE process.     

Particle shape consideration in numerical simulation of assemblies of irregularly shaped particles

The mechanical behavior of granular materials depends much on the shape of the constituent particles. Therefore appropriate modeling of particle, or grain, shape is quite important. This study employed the method of direct modeling of grain shape (Matsushima & Saomto, 2002), in which, the real shape of a grain is modeled by combining arbitrary number of overlapping circular elements which are connected to each other in a rigid way. Then, accordingly, a discrete-element program is used to simulate the assembly of grains. In order to measure the effects of grain shape on mechanical properties of assembly of grains, three types of grains—high angular grains, medium angular grains and round grains are considered where several biaxial tests are conducted on assemblies with different grain types. The results show that the angularity of grains greatly affects the behavior of granular soil.     

Thin sums matroids and duality

Building on the recent axiomatisation of infinite matroids with duality, we present a theory of representability for infinite matroids. This notion of representability allows for infinite sums, and is preserved under duality.     

Flame atomic absorption spectrometric determination of trace amounts of lead, cadmium and nickel in different matrixes after solid phase extraction on modified multiwalled carbon nanotubes

The potential of modified multiwalled carbon nanotubes (a solid-phase extraction sorbent), for the simultaneous separation and preconcentration of lead, cadmium and nickel; has been investigated. Lead, cadmium and nickel, were adsorbed quantitatively; on modified multiwalled carbon nanotubes (in the pH range of 2–4). Parameters influencing, the simultaneous preconcentration of Pb(II), Ni(II) and Cd(II) ions (such as pH of the sample, sample and eluent flow rate, type and volume of elution solution and interfering ions), have been examined and optimized. Under the optimum experimental conditions, the detection limits of this method. for Pb(II), Ni(II) and Cd(II) ions, were 0.32, 0.17 and 0.04 ng mL⁻¹ in original solution, respectively. Seven replicate determinations, of a mixture of 2.0 μg mL⁻¹ lead and nickel, and 1.0 μg mL⁻¹ cadmium; gave a mean absorbance of 0.074, 0.151 and 0.310, with relative standard deviation 1.7%, 1.5% and 1.2%, respectively. The method has been applied, to the determination of trace amounts of lead, cadmium and nickel; in biological and water samples, with satisfactory results.      

Atom interferometry with Bose-Einstein condensates in a double-well potential

A trapped-atom interferometer was demonstrated using gaseous Bose-Einstein condensates coherently split by deforming an optical single-well potential into a double-well potential. The relative phase between the two condensates was determined from the spatial phase of the matter wave interference pattern formed upon releasing the condensates from the separated potential wells. Coherent phase evolution was observed for condensates held separated by 13 microm for up to 5 ms and was controlled by applying ac Stark shift potentials to either of the two separated condensates.     

Photoinduced,Direct C(sp2)−H Bond Azo Coupling of Imidazoheteroarenes and Imidazoanilines with Aryl Diazonium Salts Catalyzed by Eosin Y

Herein, a greener approach to the eosin Y-Na₂ catalyzed, C(sp²)−H bond azo coupling of imidazoheteroarene with aryl diazonium salts is described, under acid free conditions. This direct photoredox process resulted in the corresponding azo products in good to excellent yields. Besides, this new approach could also be applicable to anilines, which is a poorly reactive substrate by other methods. The main features of this reaction are that it provides high yields and is gram-scalable and applicable to biologically relevant imidazoheteroarenes and -anilines.     

Electron Transport in Quasi‐Two‐Dimensional Porous Network of Titania Nanoparticles,Incorporating Electrical and Optical Advantages in Dye‐Sensitized Solar Cells

The integration of fast electron transport and large effective surface area is critical to attaining higher gains in the nanostructured photovoltaic devices. Here, we report facilitated electron transport in the quasi‐two‐dimensional (Q2D) porous TiO₂. Liquid electrolyte dye‐sensitized solar cells were prepared by utilizing photoanodes based on the Q2D porous substructures. Due to electron confinement in a microscale porous medium, directional diffusion toward collecting electrode is induced into the electron transport. Our measurements based on the photocurrent and photovoltage time‐of‐flight transients show that at higher Fermi levels, the electron diffusion coefficient in the Q2D porous TiO₂ is about one order of magnitude higher when compared with the conventional layer of porous TiO₂. The results show that microstructuring of the porous TiO₂ leads to an approximately threefold improvement in the electron diffusion length. Such a modification may considerably affects the electrical functionality of moderate or low performance dye‐sensitized solar cells for which the internal gain or collection efficiency is typically low.